期刊文献+

多重敏感性共聚物的制备及其自组装行为研究 被引量:6

Synthesis of multistimuli-responsive polymer and its self-assembly behavior
下载PDF
导出
摘要 采用开环聚合(ROP)和原子转移自由基聚合(ATRP)的方法合成了具有多重敏感性的聚乙二醇单甲醚-聚己内酯-聚甲基丙烯酸二乙氨基乙酯(mPEG-b-PCL-b-PDEAEMA)三嵌段共聚物,利用傅里叶变换红外光谱(FTIR)、核磁共振(NMR)和凝胶渗透色谱(GPC)对嵌段共聚物的结构及分子量进行了表征,改变投料比可有效调控各嵌段长度,所得共聚物的分子量分布均保持在1.3左右;其自组装后改变体系的pH、温度和CO2加入量可以有效控制聚集体的粒径大小,随CO2加入量的增加,粒径由238nm增大到538nm,而通入N2后其粒径大小恢复原状;对聚集体进行载药性能研究,发现CO2的加入可提高载药量及包封率,在释放阶段降低体系的pH或通入CO2可增加药物的释放速率和释放量。 In this paper, a novel multistimuli-responsive triblock copolymer poly ( ethyleneglycol )-block-poly (ε-caprolactone )-block-poly( N,N-Diethylaminoethyl methacrylate) ( mPEG-PCL-PDEAEMA) was synthesized by ROP and ATRP. The structure and molecular weight of the triblock copolymer were characterized by flourier transform infrared(FTIR),nuclear magnetic resonance (NMR)and gel permeation chromatography(GPC). The length of chain segment could be controlled by changing feed ratio and the molecular weight distribution remained at 1. 3;After self-assemble,aggregates diameter could be controlled by pH,CO2 and tempera-ture. The diameter increased from 238nm to 538nm with increasing the amount of CO2 and could recover by purging with N2. The re-sults of drug loading property experiment showed that purging with CO2 can increase the drug loading and encapsulation efficiency, in the release stage,reduce the pH and purging with CO2 can increase drug release rate and release amount.
出处 《化学研究与应用》 CAS CSCD 北大核心 2014年第3期384-389,共6页 Chemical Research and Application
基金 国家自然科学基金(51173072)资助项目 江苏省产学研联合创新资金(BY2011120)资助项目
关键词 三嵌段共聚物 自组装 多重敏感性 triblock copolymer self-assemble multistimuli-responsive
  • 相关文献

参考文献14

  • 1Jiucun Chen,Mingzhu Liu,Honghong Gong,et al. Synthesisand Self-Assembly of Thermoresponsive PEG-b-PNIPAM-b-PCL ABC Triblock Copolymer Through the Combinationof AtomTransfer Radical Polymerization, Ring-OpeningPolymerization and Click Chemistry [J]. J PhysChem B,2011,115(50):14947-14955.
  • 2Marija S Nikolic,Charlotta Olsson,Andrea Salcher,et al.Micelle and Vesicle Formation of Amphiphilic Nanoparticles[J]. Angew Chem Int,2009,48(15):2752-2754.
  • 3A Choucair,A Eisenberg. Control of Amphiphilic BlockCopolymer Morphologies Using Solution Conditions[J].Eur Phys J E,2003,10(1):37-44.
  • 4Wenling Zhang,Jinlin He,Zhuang Liu,et al. Biocompatibleand pH-Responsive Triblock Copolymer mPEG-b-PCLb-PDMAEMA:Synthesis, Self-Assembly, and Application[J]. J poly sci:part A:poly chem,2010,48 (5),1079-1091.
  • 5Loo-Teck Ng,Eiji Yuba,Kenji Kono. Modification of LiposomeSurface with pH-responsive Polyampholytes for TheControlled-release of Drugs[J]. Res Chem Intermed,2009,35(8-9):1015-1025.
  • 6Shutao Guo,Yong Qiao,Weiwei Wang,et al. Synthesis andProperties of Polycaprolactone-graft-Poly(2-(dimethylamino)ethyl Methacrylate-co-methoxy Polyethylene Glycolmonomethacrylate)as Non-viral Gene Vector[J]. Poly AdvTechnol,2011,22(12):1925-1930.
  • 7Adam Blanazs,Steven P Armes,Anthony J. Ryan. Self-AssembledBlock Copolymer Aggregates: From Micelles toVesicles and Their Biological Applications[J]. MacromolRapid Commun,2009,30(4-5):267-277.
  • 8Zacharoula Iatridi, George Mattheolabakis, KonstantinosAvgoustakis,et al. Self-assembly and Drug Delivery Studiesof pH/ thermo-sensitive Polyampholytic(A-co-B)-b-Cb-(A-co-B) Segmented Terpolymers [ J]. Soft Matter,2011,7(23):11160-11168.
  • 9郭艳玲,赵军,左榘,韩聪.嵌段共聚物核交联胶束的制备与载药性能研究[J].化学研究与应用,2008,20(6):724-728. 被引量:5
  • 10Qiang Yan,Rong Zhou,Changkui Fu,et al. CO2 -ResponsivePolymeric Vesicles That Breathe[J]. Angew ChemInt Ed,2011,50(21):4923-4927.

二级参考文献10

  • 1王彩霞,冯霞,杨军.聚合物胶束型抗癌药物给药系统研究进展[J].化学研究与应用,2006,18(6):599-602. 被引量:2
  • 2Adams ML, Lavasanifar A, Kwon GS. Amphiphilic block copolymer for drug delivery [ J ]. J. Pharma. Sci. , 2003, 92 (7) : 1343-1355.
  • 3Yokoyama M, Fukushima S, Uehara R, et al. Characterization of physical entrapment and chemical conjugation of adriamycin in polymeric miceUes and their design for in vivo delivery to a solid tumor [ J ]. J. Contr. Release, 1998, 50(1-3) :79-92.
  • 4Harada A, Togawa H, Kataoka K. Physicochemical properties and nuclease resistance of antisense- oligodeoxynucleotides entrapped in the core of polyion complex micelles composed of poly (ethylene glycol)-poly (L-lysine) block copolymers [J]. Eur. J. Pharma. Sci. , 2001, 13(1) :35-42.
  • 5IL Gyun Shin, So Yeon Kim, Young Moo Lee, et al .Methoxy poly ( ethylene glycol )/ε-caprelactone amphiphilic block copolymeric miceUe containing indomethacin. I. Preparation and characterization [ J ]. J. Contr. Release, 1998,51 : 1-11.
  • 6So Yeon Kim, IL Gyun Shin, Young Moo Lee, et al. Methoxy poly (ethylene glycol ) and ε-caprolactone amphiphilic block eopolymeric mieeUe containing indomethacin. II. Micelle formation and drug release behaviours [J]. J. Contr. Release,1998,51:13-22.
  • 7Xintao Shuai, Thomas Merdan, Andreas K. Schaper, et al. Core-Cross-Linked Polymeric Micelles as Paclitaxel Carriers [ J ]. Bioconjugate Chem. 2004,15:441-448.
  • 8Yoshinori Kakizawa, Atsushi Harada, Kazunori Kataoka. Glutathione-Sensitive Stabilization of Block Copolymer Micelles Composed of Antisense DNA and Thiolated Poly ( ethylene glycol )-block-poly ( L-lysine ) : A Potential Cartier for Systemic Delivery of Antisense DNA [ J ] . Biomacromol. , 2001,2:491-497.
  • 9Changyou Choi, Su Young Chae, Tai-Hyoung Kim, et al. Synthesis and Physicochemical Characterization of Amphiphilic Block Copolymer Self-Aggregates Formed by Poly ( ethylene glycol ) -block-Poly ( ε-caprolactone ) [ J ]. J. Appl. Poly. Sci., 2006,99:3520-3527.
  • 10Manfred Wilhelm, Cheng-Le Zhao, Yongcai Wang, et al. Poly(styrene-ethylene oxide) Block Copolymer Micelle Formation in Water: A Fluorescence Probe Study [ J]. Macromol. , 1991,24:1033-1040.

共引文献4

同被引文献89

引证文献6

二级引证文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部